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Home»Public Health Agencies»US Department of Agriculture»Kingston Pharma, LLC Issues Voluntary Recall of All Lots of “DG™ Baby Gripe Water Due to Undissolved Ingredient, Citrus Flavonoid
Kingston Pharma, LLC Issues Voluntary Recall of All Lots of “DG™ Baby Gripe Water Due to Undissolved Ingredient, Citrus Flavonoid
US Department of Agriculture

Kingston Pharma, LLC Issues Voluntary Recall of All Lots of “DG™ Baby Gripe Water Due to Undissolved Ingredient, Citrus Flavonoid

foodpoisoningnewsBy foodpoisoningnewsFebruary 15, 2019Updated:February 15, 2019No Comments2 Mins Read
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Kingston Pharma, LLC is voluntarily recalling all lots of”DG™ Baby Gripe Water herbal supplement with organic ginger and fennel extracts” into the consumer level because of the existence of an undissolved ingredient, citrus flavonoid.

Use of the product shouldn’t be considered hazardous but may lead to difficulty when consuming the product for sensitive people. Up to now, Kingston Pharma LLC has received one report of a old baby having difficulty when consuming the item and three complaints attributed to the undissolved citrus flavonoid.

The product is administered orally to babies and adults. The product is packed in 4-ounce amber bottles, white plastic caps with security seals and supplied with an oral syringe, with UPC Code 8 5495400246 3. The product was distributed throughout the USA by Dollar General Corporation.

Kingston Pharma, LLC is advising its clients by media release of the recalled product. Consumers who have merchandise that has been recalled should stop using and discard.

To report adverse reactions or quality issues experienced with the use of the product or to ask questions concerning this recall, contact Christina Condon or C. Jeanne Taborsky by telephone toll free at 844-724-7347 or from email [email protected]. Consumers should contact their doctor or health care provider if they or their child have experienced any issues that could be associated with using or taking this product.

Adverse reactions or quality issues related to the use of the product may be reported to FDA’s MedWatch Adverse Event Reporting program either by phone, on line, by regular mail or by facsimile.

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